Evaluation of the utility of the ISTH-BAT in haemophilia carriers: a multinational study

被引:75
作者
James, P. D. [1 ]
Mahlangu, J. [2 ]
Bidlingmaier, C. [3 ]
Mingot-Castellano, M. E. [4 ]
Chitlur, M. [5 ]
Fogarty, P. F. [6 ]
Cuker, A. [6 ]
Mancuso, M. E. [7 ]
Holme, P. A. [8 ,9 ]
Grabell, J. [1 ]
Satkunam, N. [1 ]
Hopman, W. M. [1 ]
Mathew, P. [10 ,11 ]
机构
[1] Queens Univ, Kingston, ON, Canada
[2] Univ Witwatersrand, Fac Hlth Sci, Johannesburg, South Africa
[3] Dr von Hauners Childrens Univ Hosp, Munich, Germany
[4] Reg Univ Hosp Malaga, Malaga, Spain
[5] Childrens Hosp Michigan, Detroit, MI 48201 USA
[6] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[7] Osped Maggiore Policlin, Angelo Bianchi Bonomi Hemophilia & Thrombosis Ctr, Fdn IRCCS Ca Granda, Milan, Italy
[8] Univ Oslo, Univ Hosp, Dept Hematol, Oslo, Norway
[9] Univ Oslo, Univ Hosp, Inst Clin Med, Oslo, Norway
[10] Bayer HealthCare, Whippany, NJ USA
[11] Univ New Mexico, Albuquerque, NM 87131 USA
关键词
bleeding; haemophilia carriers; ISTH-BAT; BLEEDING ASSESSMENT-TOOL; VON-WILLEBRAND DISEASE; A CARRIERS; FACTOR-VIII; PHENOTYPE; RANGE; DISORDERS; GENOTYPE; FEMALES; CARE;
D O I
10.1111/hae.13089
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionThere has been increasing recognition in recent years that female carriers of haemophilia manifest abnormal bleeding; however, data on the use of bleeding assessment tools in this population are lacking. AimOur objective was to validate the ISTH-BAT in haemophilia carriers to describe bleeding symptoms and allow for comparisons with factor levels and other patient groups. MethodsThis was a prospective, observational, cross-sectional study performed by members of Global Emerging HEmostasis Panel(GEHEP). Unselected consecutive haemophilia carriers were recruited and a CRF and the ISTH-BAT were completed by study personnel. ResultsA total of 168 haemophilia carriers were enrolled: 155 haemophilia A and 13 haemophilia B. The mean age was 40years (range: 20-82). Carriers had higher mean bleeding scores (BS) compared with age-matched controls (n=46; 5.7 vs. 1.43; P<0.0001) and Type 3 VWD OC (n=32; 3.0; P=0.009), but lower BS compared with women with Type 1 VWD (n=83; 8.7; P<0.0001). Fifteen carriers reported haemarthrosis, and of those six had normal FVIII/FIX levels. There was a significant but weak negative correlation between BS and factor level (Spearman's r(2)=-0.36, P<0.001). ConclusionOur results show that haemophilia carriers experience abnormal bleeding, including haemarthrosis. Overall, BS in women with Type 1 VWD>haemophilia carriers>Type 3 VWD OC>controls. Understanding the performance of the ISTH-BAT in this population is a critical step in future research aimed at investigating the underlying pathophysiology of abnormal bleeding, with the ultimate goal of optimizing treatment.
引用
收藏
页码:912 / 918
页数:7
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